RecruitingPHASE2, PHASE3NCT06581406

A Randomized, Phase 2/3 Study to Investigate the Efficacy and Safety of RP2 in Combination With Nivolumab in Immune Checkpoint Inhibitor-Naïve Adult Patients With Metastatic Uveal Melanoma

Studying Uveal melanoma

Last synced from ClinicalTrials.gov

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Key facts

Sponsor
Replimune Inc.
Principal Investigator
Rahul Marpadga, MD MPH
Replimune Inc.
Intervention
RP2(biological)
Enrollment
280 enrolled
Eligibility
All sexes
Timeline
20242031

Study locations (30)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT06581406 on ClinicalTrials.gov

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